Drug: |
||||
---|---|---|---|---|
Trial Name: |
Study Of PI3K/mTOR Inhibitors In Combination With A MEK Inhibitor Or Irinotecan In Patients With Advanced Cancer |
|||
NCT#: |
||||
Conditions: |
Solid Tumors |
|||
Status: |
Terminated |
|||
Phase: |
1 |
Start Date 10/01/2011 |
Age of Trial (yrs) 13.5 |
|
Treatment Phase: |
Gleevec-resistant |
|||
Drug Category: |
PI3K/mTOR inhibitor + MEK inhibitor + TOPO-1 inhibitor |
|||
Strategy: |
Block related tumor signal paths |
|||
Trial Type: |
GIST not specified. GIST patient enrollment unknown. |
|||
Other Protocol IDs: |
B1271002 |
|||
Sponsor: |
Pfizer |
|||
Patient Contact: |
Pfizer CT.gov Call Center
1-800-718-1021
Pfizer Oncology Clinical Trial Information Service
1-877-369-9753
PfizerCancerTrials@emergingmed.com |
|||
Contact email: |
||||
Contact Phone: |
||||
Randomized: |
||||
IV or Oral: |
Oral
Intravenous |
|||
Trial Notes: |
Purpose: After the second protocol amendment two study arms are evaluated in this clinical protocol: PD-0325901 (MEK inhibitor) plus PF-05212384 (PI3K/mTOR inhibitor) and PF-05212384 plus irinotecan. The study will assess safety, pharmacokinetics and pharmacodynamics of these combinations in patients with advanced cancer. Once the maximum tolerated doses are identified, further assessment of these combinations will be done in patients with previously treated metastatic colorectal cancer or pancreatic cancer for the PF-05212384 plus irinotecan arm and in patients with KRAS mutated colorectal cancer for the combination of PF-05212384 plus PD-0325901 |
Trial Links |
Trial Results |
Drug Information |
Name |
Address |
City |
State |
Zip |
Country |
10945 Le Conte Ave. |
Los Angeles |
CA |
90095 |
USA |
|
1665 N. Ursula St. |
Aurora |
CO |
80045 |
USA |
|
610 University Ave |
Toronto |
ON |
M5G 2M9 |
Canada |
|
119-129 |
Barcelona |
08035 |
Spain |
||
Milan |
20132 |
Italy |
|||
2020 Santa Monica Boulevard Suite 600 |
Santa Monica |
CA |
90404 |
USA |
|
Charleston |
SC |
29425 |
USA |